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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080311Generated: November 2, 2026

Triethylamine → tert-Butyl 4-[(3-bromophenyl)methyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/2080311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Bromobenzyl bromideHCID 69979—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium BicarbonateHCID 516892—
SolventAcetonitrileHCID 6342—
Producttert-Butyl 4-[(3-bromophenyl)methyl]piperazine-1-carboxylateHCID 5343921289.7%

Reaction Steps

A solution of 3-bromobenzyl bromide (6 g) and Boc-piperazine (4.06 g) in acetonitrile (30 mL) was treated with triethylamine (3.36 mL). The resulting mixture was heated at reflux for 16 hours. After cooling to room temperature, the reaction mixture was treated with saturated sodium bicarbonate solution (20 mL), and then extracted with ethyl acetate (2×30 mL). The organic phases were combined, dried (MgSO4) and concentrated under vacuum. The residue was purified by chromatography on silica (100 g) eluting with ethyl acetate/cyclohexane to give the title compound (6.95 g). LC/MS: m/z, 355, 357 (M+H), 2.40 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932247B2
Source datasetuspto-grants-2011_04
ORD IDord-fca5d91c9e904a32ac6bd6a954f349c8
Source noteuspto-grants-2011_04